Canonical Allele Identifier: CA2841603626

Gene: PTPRG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.62079038C>T , CM000665.2:g.62079038C>T	GRCh38
NC_000003.11:g.62064712C>T , CM000665.1:g.62064712C>T	GRCh37
NC_000003.10:g.62039752C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474889.6:c.615+780C>T MANE Select	ENSP00000418112.1:n.615+780C>T
ENST00000295874.14:c.615+780C>T	ENSP00000295874.10:n.615+780C>T
ENST00000474889.5:c.615+780C>T	ENSP00000418112.1:n.615+780C>T
ENST00000615556.3:c.429+780C>T	ENSP00000484346.1:n.429+780C>T
ENST00000618938.2:c.429+780C>T	ENSP00000480407.1:n.429+780C>T
NM_002841.3:c.615+780C>T	NP_002832.3:n.615+780C>T
XM_005265352.3:c.573+780C>T	XP_005265409.1:n.573+780C>T
XM_005265353.3:c.615+780C>T	XP_005265410.1:n.615+780C>T
XM_017006961.2:c.735+780C>T	XP_016862450.1:n.735+780C>T
XM_017006962.1:c.654+780C>T	XP_016862451.1:n.654+780C>T
XM_017006963.2:c.735+780C>T	XP_016862452.1:n.735+780C>T
XM_017006964.1:c.267+780C>T	XP_016862453.1:n.267+780C>T
NM_002841.4:c.615+780C>T MANE Select	NP_002832.3:n.615+780C>T
NM_001375471.1:c.615+780C>T	NP_001362400.1:n.615+780C>T